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Under the Premarket Tobacco Product Application (PMTA) scheme, the FDA is responsible for assessing and authorizing the sale of new tobacco products, and determines, based on the assessment of the scientific evidence, whether new tobacco products are appropriate for the protection of the public health with respect to the risks and benefits to the population as a whole, considering both users and nonusers

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With the federal government out of the picture, the need for civil society engagement has never been greater

Protecting Smokers, Saving Lives: The Case for a Tobacco and Nicotine Regulatory Authority

Non-slip rolling tray : Keeps your space tidy, prevents spills, and makes it easier to organize your tools